Explore Workflows
View already parsed workflows here or click here to add your own
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find_hotspots_in_normals.cwl
Workflow to find hotspot VAFs from duplex (for Tumor sample) and unfiltered (for Normal sample) pileups. These inputs are all required to be sorted in the same order: sample_ids patient_ids sample_classes unfiltered_pileups duplex_pileups |
Path: workflows/subworkflows/find_hotspots_in_normals.cwl Branch/Commit ID: master |
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cnv_gridss
CNV GRIDSS calling |
Path: structuralvariants/cwl/subworkflows/cnv_gridss.cwl Branch/Commit ID: 1.0.7 |
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scRNA-seq pipeline using Salmon and Alevin
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Path: pipeline.cwl Branch/Commit ID: f8ea70d |
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cnv_exomedepth
CNV ExomeDepth calling |
Path: structuralvariants/cwl/subworkflows/cnv_exome_depth.cwl Branch/Commit ID: 1.1.3 |
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01-qc-pe.cwl
ChIP-seq 01 QC - reads: PE |
Path: v1.0/ChIP-seq_pipeline/01-qc-pe.cwl Branch/Commit ID: master |
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scatter GATK HaplotypeCaller over intervals
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Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: No_filters_detect_variants |
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Detect Variants workflow
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Path: detect_variants/detect_variants.cwl Branch/Commit ID: master |
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count-lines17-wf.cwl
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Path: tests/count-lines17-wf.cwl Branch/Commit ID: main |
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count-lines2-wf.cwl
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Path: v1.0/v1.0/count-lines2-wf.cwl Branch/Commit ID: master |
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cat_fastq.cwl
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Path: python/lib/MICGENT/data/cwl/cat_fastq.cwl Branch/Commit ID: master |
